5-[(2E)-4-methoxybut-2-en-1-yl]-4-methyl-2-nitro-N-(3-phenylpropyl)aniline

Base Information

Chemical Name:5-[(2E)-4-methoxybut-2-en-1-yl]-4-methyl-2-nitro-N-(3-phenylpropyl)aniline
CAS No.:1338684-21-1
Molecular Formula:C₂₁H₂₆N₂O₃
Molecular Weight:354.449
Hs Code.:

Synonyms:5-[(2E)-4-methoxybut-2-en-1-yl]-4-methyl-2-nitro-N-(3-phenylpropyl)aniline

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 5-[(2E)-4-methoxybut-2-en-1-yl]-4-methyl-2-nitro-N-(3-phenylpropyl)aniline

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Technology Process of 5-[(2E)-4-methoxybut-2-en-1-yl]-4-methyl-2-nitro-N-(3-phenylpropyl)aniline

There total 5 articles about 5-[(2E)-4-methoxybut-2-en-1-yl]-4-methyl-2-nitro-N-(3-phenylpropyl)aniline which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 58.0%

: 627-40-7
methylallylether

: 1338684-20-0
5-allyl-4-methyl-2-nitro-N-(3-phenylpropyl)aniline

: 1338684-21-1
5-[(2E)-4-methoxybut-2-en-1-yl]-4-methyl-2-nitro-N-(3-phenylpropyl)aniline

Guidance literature:: With camphor-10-sulfonic acid; In dichloromethane; at 20 ℃; for 18h; Inert atmosphere;

Reference yield:

: 40371-61-7
N-(3-bromo-4-methyl-phenyl)acetamide

: 1338684-21-1
5-[(2E)-4-methoxybut-2-en-1-yl]-4-methyl-2-nitro-N-(3-phenylpropyl)aniline

Guidance literature:: Multi-step reaction with 5 steps

1.1: nitric acid / water / 2 h / 50 °C

2.1: hydrogenchloride / water / 3 h / 70 °C

2.2: pH 10

3.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0.5 h / 0 - 20 °C

3.2: 20 °C

4.1: bis-triphenylphosphine-palladium(II) chloride / N,N-dimethyl-formamide / 0.42 h / Inert atmosphere

4.2: 3 h / 105 °C / sealed tube

5.1: camphor-10-sulfonic acid / dichloromethane / 18 h / 20 °C / Inert atmosphere

With hydrogenchloride; camphor-10-sulfonic acid; nitric acid; sodium hydride; bis-triphenylphosphine-palladium(II) chloride; In dichloromethane; water; N,N-dimethyl-formamide; mineral oil;

Reference yield:

: 40371-62-8
acetic acid-(5-bromo-4-methyl-2-nitro-anilide)

: 1338684-21-1
5-[(2E)-4-methoxybut-2-en-1-yl]-4-methyl-2-nitro-N-(3-phenylpropyl)aniline

Guidance literature:: Multi-step reaction with 4 steps

1.1: hydrogenchloride / water / 3 h / 70 °C

1.2: pH 10

2.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0.5 h / 0 - 20 °C

2.2: 20 °C

3.1: bis-triphenylphosphine-palladium(II) chloride / N,N-dimethyl-formamide / 0.42 h / Inert atmosphere

3.2: 3 h / 105 °C / sealed tube

4.1: camphor-10-sulfonic acid / dichloromethane / 18 h / 20 °C / Inert atmosphere

With hydrogenchloride; camphor-10-sulfonic acid; sodium hydride; bis-triphenylphosphine-palladium(II) chloride; In dichloromethane; water; N,N-dimethyl-formamide; mineral oil;